Material Handler - All Shifts

About the role

Join a high-impact team that keeps life-changing biopharmaceutical manufacturing running smoothly. As a Material Handler, you’ll be the engine behind safe, compliant, and efficient material flow across GMP cleanroom environments—ensuring production teams have exactly what they need, when they need it. If you thrive in a fast-paced, highly regulated setting and take pride in precision, this is your opportunity at FUJIFILM Biotechnologies in Holly Springs, North Carolina.

About the company

FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By the end of 2025, we’ll open North America’s largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof. We’re looking for passionate, mission-driven people to help us realize this vision and deliver the next vaccine, cure, or therapy.

Holly Springs combines small-town warmth with proximity to Raleigh’s thriving tech scene, offering the perfect blend of community and opportunity. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across healthcare, electronics, business innovation, and imaging segments. We are guided by our Group Purpose of “giving our world more smiles.”

Responsibilities

• Perform routine and periodic cleaning of manufacturing areas from Grade Controlled Non-Classified (CNC) through Grade C environments, including ceilings, walls, floors, surfaces, and equipment exteriors using approved agents.
• Execute material movements and transactions in SAP (or similar ERP): goods receipt, staging, transfer, consumption, and inventory adjustments.
• Receive, inspect, and verify incoming materials against purchase orders and documentation.
• Stage and deliver raw materials, consumables, and components to manufacturing in alignment with production schedules.
• Maintain accurate inventory levels; support cycle counts and reconciliation activities.
• Ensure proper labeling, status identification, and segregation of materials (released, quarantined, rejected).
• Complete required training and maintain compliance for Hazardous Waste Disposal.
• Wipe down and transfer materials into CNC through Grade C areas following approved disinfection procedures; adhere to gowning requirements and aseptic practices.
• Complete all required documentation in compliance with GMP and GDP standards; maintain accurate, real-time records of material movements and transactions.
• Follow SOPs, batch records, and work instructions with exceptional attention to detail.
• Operate material handling equipment (e.g., pallet jacks, forklifts) safely and per site procedures.
• Maintain cleanliness and organization of warehouse and staging areas using 5S principles; perform routine cleaning of workspaces and equipment.
• Collaborate with Manufacturing, Quality, and Supply Chain to ensure timely material availability.
• Support production campaigns by ensuring continuous material flow to prevent downtime.
• Assist with deviation investigations related to materials, as applicable.
• Perform other duties as assigned.

Requirements

• High school diploma or equivalent required with 1–3 years of experience in a GMP-regulated environment (biopharma, pharmaceutical, or medical device preferred); OR Associate’s degree with 0–1 years of experience in a GMP-regulated environment (biopharma, pharmaceutical, or medical device preferred).
• Experience with SAP or similar ERP systems.

Preferred Qualifications

• Associate’s degree, preferably in Life Sciences or a related field.
• 2+ years of direct experience in a cGMP manufacturing environment.

Skills

• Proficiency in ERP or Warehouse Management Software.
• Basic computer skills (SAP, Microsoft Office).
• Strong problem-solving, organizational, and time management skills.
• Strong leadership and decision-making abilities.
• Experience with advanced warehouse automation and optimization tools.
• Ability to manage high-volume material operations.

Benefits

• Purposeful work: Help enable the production of critical therapies by ensuring flawless material flow.
• Growth and learning: Expand your GMP, cleanroom, and ERP expertise in a collaborative environment.
• Culture of excellence: Join a team that values safety, quality, accuracy, and continuous improvement.